U.S. patent number 5,628,888 [Application Number 08/624,720] was granted by the patent office on 1997-05-13 for apparatus for electrochemical treatment of water and/or water solutions.
This patent grant is currently assigned to RSCECAT, USA, Inc.. Invention is credited to Vitold M. Bakhir, Taras Barabash, Jury G. Zadorozhny.
United States Patent |
5,628,888 |
Bakhir , et al. |
May 13, 1997 |
Apparatus for electrochemical treatment of water and/or water
solutions
Abstract
An apparatus for electrochemical purification of water and for
regulation of acid-alkaline properties, Red-Ox characteristics and
catalytic activity of water that can be used for obtaining washing
and disinfecting solutions. The apparatus includes at least one
electrochemical cell which contain vertical coaxial cylindrical and
rod electrodes made from material nonsoluble during electrolysis
and an ultrafiltration ceramic diaphragm installed in the bushings
between the electrodes to create inter-electrode space in the
electrode chambers. The lower and upper bushings have a channels
for the treated solution supply into and discharge from the
electrode chambers. The channels are connected to the feeding and
discharging adjustment lines. There is also a metering pump on the
water line for sodium chloride dosing into the water to be treated.
The water line contains a flow regulator connected to the feeding
and discharging adjustment lines. Poles of the power supply are
connected to the electrodes. The feeding line is connected to the
inlet of the negative electrode chamber and the output of the
negative electrode chamber is connected to the inlet of the
positive electrode chamber by a special line which has an
adjustment for discharging a part of the degasified treated
solution from the chamber of the negative electrode. A catalyst
chamber can be installed on the special line. The catalyst chamber
contains a mixture of particles of carbon and manganese dioxide. A
separator with a tangential inlet is used for discharging a part of
the degasified processed solution.
Inventors: |
Bakhir; Vitold M. (Moscow,
RU), Zadorozhny; Jury G. (Moscow, RU),
Barabash; Taras (Moscow, RU) |
Assignee: |
RSCECAT, USA, Inc. (Las Vegas,
NV)
|
Family
ID: |
26653692 |
Appl.
No.: |
08/624,720 |
Filed: |
March 28, 1996 |
Current U.S.
Class: |
204/260; 204/263;
204/295 |
Current CPC
Class: |
C02F
1/4674 (20130101); C02F 1/4618 (20130101); C25B
9/19 (20210101); C02F 2001/46152 (20130101); C02F
2201/46115 (20130101); C02F 1/001 (20130101); C02F
2201/003 (20130101); C02F 2303/04 (20130101); C02F
2001/46138 (20130101); C02F 2201/4611 (20130101); C02F
2209/04 (20130101); C02F 2209/06 (20130101); C02F
2201/4618 (20130101) |
Current International
Class: |
C02F
1/467 (20060101); C02F 1/461 (20060101); C25B
9/08 (20060101); C25B 9/06 (20060101); C25B
009/00 (); C25B 013/04 () |
Field of
Search: |
;204/260,295,263 |
References Cited
[Referenced By]
U.S. Patent Documents
Primary Examiner: Valentine; Donald R.
Attorney, Agent or Firm: Roethel; John Edward
Claims
We claim:
1. An apparatus for obtaining washing and disinfecting solutions by
means of electrolysis of a sodium chloride water solution, the
apparatus comprising:
a) at least one electrochemical cell which contains vertical
coaxial cylindrical and rod electrodes and a diaphragm, each of
which are made from material which is nonsoluble during
electrolysis; each of the electrodes mounted in dielectric bushings
and connected to the poles of a power supply;
b) the diaphragm comprising an ultrafiltration ceramic diaphragm
made from a base material of zirconium oxide and installed between
the electrodes; the diaphragm separating an inter-electrode space
into a negative electrode chamber and a positive electrode
chamber;
c) the dielectric bushings comprising a lower bushing and an upper
bushing, each having a channel for the treated solution supply into
and discharge from the electrode chambers; the channels being
connected to a feeding line and a discharge line;
d) a feeding line connected to an inlet of the negative electrode
chamber, the feeding line comprising a water line and a sodium
chloride dosing line, the feeding line further including a metering
pump on the water line for dosing the sodium chloride into the
water to be treated;
e) the water line further containing a flow regulator connected to
the feeding and discharging adjustments; and
f) an outlet of the negative electrode chamber being connected to
an inlet of the positive electrode chamber by a special line, the
special line having an adjustment for discharging a part of a
degasified processed solution from the negative electrode
chamber.
2. The apparatus as claimed in claim 1 further comprising a
catalyst chamber mounted on the special line for providing
catalyst.
3. The apparatus as claimed in anyone of claims 1-2 wherein the
catalyst chamber contains a mixture of particles of carbon and
manganese dioxide.
4. The apparatus as claimed in anyone of claims 1-3 wherein the
adjustment for discharging a part of the degasified processed
solution is executed as a separator with a tangential inlet.
5. The apparatus as claimed in anyone of claims 1-4 wherein the
adjustments for the feeding and discharging of treated solution are
executed as a collectors for parallel joining of two and more
cells.
Description
This invention relates to the area of chemical technology, and more
particularly to apparatus for the electrochemical treatment and
purification of water and/or water solutions and for the regulation
of acid-alkaline properties, Red-Ox characteristics and catalytic
activity of water and can be used for obtaining
washing/disinfecting solutions.
BACKGROUND OF THE INVENTION
In the area of applied electrochemistry, different design
electrolyzers have been used for water treatment or for obtaining
washing and disinfecting solutions.
A device with flat perforated electrodes pressed against the
diaphragm is used for water treatment in the anode chamber and
cathode chamber separately. See the Author's Certificate USSR No.
882944 (1978). One of the disadvantages of such a device is the
poor hydrodynamics. Another disadvantage is that the resulting
products from the anode electrochemical reaction and the cathode
electrochemical reaction can become mixed together because the
diaphragm has a high penetrability. Also such an electrolyzer
containing flat electrodes requires excessive manual labor in order
to be assembled and repaired.
Another device for the electrolysis of water consists of a
cylindrical electrolyzer with coaxial electrodes which are fixed in
dielectric bushings and a diaphragm is placed between the
electrodes. The diaphragm separates the inter-electrode space in
the cathode and anode chambers. See Japanese Published Patent
Application No. 1-104387 (1989). Each chamber has a separate inlet
in the lower bushing and a separate outlet in the upper bushing of
the electrolyzer which are connected to the pressurized water line.
The device includes a power supply connected to the electrodes
through the switchboard for changing the polarity of electrodes,
for descaling of the cathode electrode and for switching the
hydraulic lines which provide the solution output from the anode
chamber and the cathode chamber without mixing of the resulting
solutions. It is possible to obtain electrochemical processed water
with biocide characteristics by using this device.
The disadvantage of this device is the high energy consumption
required for water treatment, in particular for the treatment of
water which is changing its mineralization during the treatment.
The broader the range of mineralization change attempted, the more
powerful must be the power supply.
The device that is closest by the technical design and achieved
result to the present invention is the apparatus for
electrochemical treatment of water discloses in U.S. Pat. No.
5,427,667 (Bakhir et al.), which is a prototype from which the
present invention evolved. The device disclosed in this application
contains at least one electrochemical cell. The cell contains
vertical coaxial cylindrical and rod electrodes and a diaphragm,
each of which are made from material which is nonsoluble during
electrolysis. The electrodes are installed in dielectric bushings.
An ultrafiltration ceramic diaphragm, the main ingredient of which
is zirconium oxide, is installed in the bushings between the
electrodes. The ability to change the geometric dimensions of the
cell is limited by the formula.
The cells are fastened in the lower and upper collectors which are
made from dielectric material. The collectors have channels for
incoming and outgoing solutions. The cells are installed in the
collectors in parallel hydraulically and in parallel or in
series--parallel electrically.
The electrodes of the cell are connected with the poles of the
power supply in such a way that the cylindrical electrode is an
anode and the rod electrode is a cathode. Both electrode chambers
are connected with the incoming water in a parallel manner and the
cell has flow regulators on both lines. The device also has a
water-jet pump for dosing a reagent entered from the tank installed
on the water supplying line. The device may include a catalytic
chamber. The power supply connected to the electrodes through the
switchboard. The anode treated solution is a disinfectant and the
cathode treated solution is a washing solution. The disadvantages
in using this device for water treatment are that it requires
relatively high power consumption and a large number of reagents to
clean the cells.
The object of the present invention is to provide an improved
apparatus for electrochemical treatment of water that reduces power
consumption and extends the functional abilities of the earlier
devices. This is achieved by varying the parameters of anolyte and
catholyte, in particular by increasing the biocide characteristics
of anolyte and reducing its corrosion activity.
This object can be achieved when the device for obtaining washing
and disinfecting solutions by the electrolysis of sodium chloride
water solution contains at least one electrochemical cell. The cell
contains vertical coaxial cylindrical and rod electrodes made from
material that is nonsoluble during electrolysis, and a coaxial
ceramic ultrafiltration diaphragm. The cylindrical and rod
electrodes are installed in the dielectric bushings. The ceramic
ultrafiltration diaphragm is installed in the bushings between the
electrodes. The diaphragm separates the inter-electrode space into
two chambers.
Lower and upper bushings have channels for the treated solution
that is supplied into and is discharged from the electrode
chambers. The device also contains a metering pump for introducing
sodium chloride to the treated water. The water line has a flow
regulator which is connected to the metering pump. The poles of the
power supply are connected to the electrodes. The feeding line is
connected to the inlet of the negative electrode chamber. The
outlet of the negative electrode chamber is connected to the inlet
of the positive electrode chamber by a special line which has an
adjustment for discharging part of the degasified processed
solution from the chamber of the negative electrode. In addition, a
chamber with catalyst can be installed on the special line. The
catalytic chamber may contain a mixture of carbon and manganese
oxide and has an inlet in the upper part and an outlet in the lower
part. The adjustment for discharging part of the degasified
processed solution is executed, for instance, as a separator with
the tangential inlet containing a valve which permits the discharge
of part of the flow and, after degasification, sends it to the end
user. The adjustments for supplying and discharging the treated
solution are made as collectors which permits the joining of two or
more cells.
It is a known method when the treated solution is consequently
passed first through the cathode chamber and then through the anode
chamber. See, for instance, Inventor's Certificate USSR No. 865829
(1980). The order of water flowing through the electrode chambers
is defined by the requirements for the purification rate from the
ions of heavy metals. The regulation of the processes, which are
ongoing in the electrode chambers, is aimed of changing the pH of
the treated solution. These changes are significant in comparison
with the initial solution. In particular, the pH of the solution
treated in the cathode chamber is changed so that the treated
solution produces a high alkaline reaction which exceeds the pH
value for the hydrate formation. In order to obtain a neutral pH,
after the filtration of the nonsoluble hydroxides, the
acidification of the cathode treated water in the anode chamber is
required.
With the new device of the present invention, it is essential that
the cathode treated solution together with hydrogen flows through
the anode chamber. Regulation of the pH is not so important due to
the small value pH changes achieved. The main results from the
process are the reduction-oxidizing (Red-Ox) reactions taking place
on the surfaces of electrodes and in the volume of the solution.
Red-Ox reactions permit the producing of washing and disinfecting
solutions with the required characteristics.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 shows one of the preferred embodiments of the present
invention for the electrochemical synthesis of washing and
disinfecting solutions in which the negative chamber outlet is
connected with the positive chamber inlet by the special line.
FIG. 2 shows schematically the preferred embodiment of the present
invention of FIG. 1.
FIG. 3 shows another preferred embodiment of the present invention
for the electrochemical synthesis of washing and disinfecting
solutions in which a catalyst chamber is provided on the special
line.
FIG. 4 shows schematically the preferred embodiment of the present
invention of FIG. 3.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
The present invention is an improvement on the prototype apparatus
for electrochemical treatment of water disclosed in U.S. Pat. No.
5,427,667, the disclosure of which is incorporated herein by this
reference thereto.
The apparatus of the present invention for obtaining washing and
disinfecting solutions is shown in FIGS. 1 and 2 and contains an
electrochemical cell 1. The electrochemical cell is described in
connection with the prototype in U.S. Pat. No. 5,427,667. The
vertical coaxial electrodes (anode and cathode) of the cell are
connected to the poles of the power supply (not shown). The ceramic
diaphragm is made from zirconium oxide, aluminum oxide and yttrium
oxide, is installed between the electrodes and separates the
inter-electrode space in the electrode chambers: the anode chamber
2 and the cathode chamber 3. The cathode chamber 3 is connected to
the feeding line 4 containing the solution to be treated. This line
also contains the running water line 5 and the brine line 6. The
running water line 5 contains a filter 7 and the brine line 6
contains a filter 8 to remove impurities. The brine line 6 contains
the valve 9. The negative electrode chamber outlet 3 is connected
to the inlet of the positive electrode chamber 2 by the special
line 10. The special line 10 contains an adjustment 11. The
adjustment 11 permits the discharge of part of the degasified
treated solution from the negative electrode chamber 3. The
adjustment 11 can be made, for example, as a separator with the
tangential inlet containing a valve type device 12 for discharging
part of the treated solution and, after degasification, delivering
it to the user.
As shown in FIGS. 3 and 4, the special line 10 may also have a
chamber 13 containing the catalyst. The chamber 13 can contain, for
instance, a mixture of particles of carbon and manganese dioxide.
The catalyst allows one to control changes in the anolyte
properties (reducing its corrosion activity) by regulation of the
content of active ingredients in the catholyte.
The apparatus of the present invention works as follows. Source
solution runs in line 4 and contains water filtered 7 from the
impurities line 5 and a solution of sodium chloride carried in line
6. The water and sodium chloride proportions in the source solution
can be adjusted by the valve 9. The source solution , enters into
the cathode chamber 3 of the electrochemical cell 1. The amount of
sodium chloride in the water depends upon the application. When the
power supply is on, the position of the valve 12 affects how the
process is run.
If the valve 12 is closed, the entire volume of the catholyte,
together with the hydrogen, which was produced during electrolysis,
enters into the anode chamber 2 of the electrochemical cell 1.
Chemical Reactions:
As a result, the anolyte increases its biocidal activity and
decreases its corrosion activity (pH=7.2-7.6).
If the valve 12 is opened slightly and part of the catholyte is
discharged, then the specific electric output for making anolyte is
increased. ##STR1## where: I=current (A)
Q.sub.total =flow through the device
Q.sub.catholyte =catholyte output
With reference to FIGS. 3 and 4, adding the catalyst chamber 13
makes it possible to neutralize a portion of the active ingredients
in the catholyte and to increase the efficiency in the anode
chamber 2, since part of the current, which was used earlier for
the neutralization of active ingredients in the catholyte, assists
in changing the characteristics of the anolyte. This allows one to
increase the biocidal activity of the anolyte without measurably
changing the pH.
The invention is illustrated by the following example, which is not
intended to exhaust all of its possibilities.
EXAMPLE
The cell contains titaniun electrodes coated with platinum or
platinum-iridium and a ceramic ultrafiltration diaphragm (see U.S.
Pat. No. 5,427,667) was used for water treatment. The concentration
of sodium chloride in the initial solution was 2 g/l. The power
consumption was 1.8 KWHR/l.
The valve 12 was closed and the whole solution is run from the
cathode chamber 3 into the anode chamber 2 together with the free
hydrogen. The biocidal activity of the obtained anolyte was from 16
min. The corrosion activity of the obtained anolyte was 1.0
mm/year.
(Biocidal activity was determined by the time (minutes) required
for disinfecting 1 liter of water containing bacteria of E coli
group in concentrations of 1.107 after 1 ml of the anolyte, with
the concentration of active chlorine 300 ppm added.)
The level of corrosion activity was determined by the velocity of
the corrosion of metal samples (St. 3) using the weight method arid
was recalculated on the standard factor: a millimeter per
annum).
Anolyte has the following parameters:
pH=8.5;
ORP=+780 mV comparatively to the chlorine-silver electrode.
When the valve 12 was opened and part of the catholyte (10% from
the whole volume) was discharged, anolyte had the following
parameters:
biocidal activity--13 minutes;
corrosion activity--1.9 mm/year;
pH=6.5;
ORP=+860 mV comparatively to the chlorine-silver electrode.
The catholyte (which can be used as a washing agent) was obtained
with the following parameters: pH=11.0; ORP=-750 mV.
When using the catalytic carbon-manganese dioxide chamber on the
special line, anolyte with the following characteristics was
obtained:
______________________________________ without catholyte with 10%
of the Characteristics discharging catholyte discharged
______________________________________ Biocidal activity 14 min. 12
min. Corrosion activity 1.8 mm/year 3.1 mm/year pH 8.0 6.0 ORP +800
mV +920 mV ______________________________________
The above results can be compared to the characteristics of the
anolyte and catholyte which can be obtained using the prototype
apparatus disclosed in U.S. Pat. No. 5,427,667:
______________________________________ Characteristics Anolyte
Catholyte ______________________________________ Biocidal activity
12-20 min. Corrosion activity 3.5-10 mm/year pH 3.8-6.0 9.5-12.0
ORP +780-+960 mV -600--800 mV
______________________________________
In accordance with the data presented herein, the invention allows
one to obtain a bactericidal solution (anolyte) with wider
functional abilities than in the prototype apparatus disclosed in
U.S. Pat. No. 5,427,667. The present invention provides a
possibility of fine regulation of the anolyte parameters during the
process. The present invention also provides a possibility to
increase a bactericidal activity of the anolyte and decrease its
corrosion activity at the same time.
* * * * *